omimdefinitions
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| Spastic ataxia, Charlevoix-Saguenay type, 270550 (3)
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| Muscular dystrophy, limb-girdle, type 2C, 253700 (3)
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| {Dermatitis, atopic, susceptibility to, 5} (2)
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| Pulmonary hypertension, primary, 2, 615342 (3)
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| Pancreatic agenesis, 260370 (3)
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| MODY, type IV, 606392 (3)
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| * 600733 PANCREAS/DUODENUM HOMEOBOX PROTEIN 1| PDX1
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| {Attention deficit-hyperactivity disorder, susceptibility to, 6} (2)
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| Fibrosis of extraocular muscles, congenital, 3C (2)
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| * 604242 RING FINGER PROTEIN 6| RNF6
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| Myopia 20, autosomal dominant (2)
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| Microcephaly 6, primary, autosomal recessive, 608393 (3)
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| Seckel syndrome 4, 613676 (3)
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| Treacher Collins syndrome 2, 613717 (3)
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| Hypotrichosis 12, 615885 (3)
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| ?Moebius syndrome (2)
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| Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria), 612073 (3)
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| Peters-plus syndrome, 261540 (3)
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| {Breast-ovarian cancer, familial, 2}, 612555 (3)
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| Fanconi anemia, complementation group D1, 605724 (3)
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| * 600185 BRCA2 GENE| BRCA2
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| {Breast cancer, male, susceptibility to}, 114480 (3)
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| Wilms tumor, 194070 (3)
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| {Medulloblastoma}, 155255 (3)
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| {Glioblastoma 3}, 613029 (3)
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| {Pre-B-cell acute lymphoblastic leukemia} (3)
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| Pancreatic cancer, 613347 (3)
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| Keratosis linearis with ichthyosis congenita and sclerosing keratoderma, 601952 (3)
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| Troyer syndrome, 275900 (3)
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| [Protein Z deficiency], 614024 (3)
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| Enuresis, nocturnal, 1 (2)
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| Hypophosphatemic rickets and hyperparathyroidism (2)
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| Cryptorchidism, 219050 (3)
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| Congenital disorder of glycosylation, type IIl, 614576 (3)
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| Shaheen syndrome, 615328 (3)
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| * 608945 FRAS1-RELATED EXTRACELLULAR MATRIX PROTEIN 2| FREM2
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| {Inflammatory bowel disease 27} (2)
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| Polydactyly, postaxial, type A5 (2)
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| [Body mass index QTL2] (2)
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| [Bone mineral density QTL 9] (2)
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| {Leukemia, chronic lymphocytic, susceptibility to, 2} (2)
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| Chromosome 13q14 deletion syndrome (4)
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| Gastroesophageal reflux (2)
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| Dementia, familial British, 176500 (3)
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| Dementia, familial Danish, 117300 (3)
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| * 607867 RCC1 DOMAIN- AND BTB DOMAIN-CONTAINING PROTEIN 1| RCBTB1
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| {Alcohol dependence, susceptibility to}, 103780 (3)
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| * 601861 REGULATORY FACTOR X-ASSOCIATED PROTEIN| RFXAP
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| Rieger syndrome, type 2 (2)
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| Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3)
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| Spastic paraplegia 24, autosomal recessive (2)
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| Osteopetrosis, autosomal recessive 2, 259710 (3)
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| * 182135 5-@HYDROXYTRYPTAMINE RECEPTOR 2A| HTR2A
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| {Obsessive-compulsive disorder, susceptibility to}, 164230 (3)
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| {Seasonal affective disorder, susceptibility to}, 608516 (3)
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| {Alcohol dependence, susceptibility to}, 103780 (3)
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| {Anorexia nervosa, susceptibility to}, 606788 (3)
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| {Major depressive disorder, response to citalopram therapy in}, 608516 (3)
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| * 136533 FORKHEAD BOX O1A| FOXO1A
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| * 607796 PHD FINGER PROTEIN 11| PHF11
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| {Asthma}, 600807 (3)
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| Aicardi-Goutieres syndrome 2, 610181 (3)
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| Retinoblastoma, 180200 (3)
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| Osteosarcoma, somatic, 259500 (3)
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| * 614041 RB1 GENE| RB1
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| Small cell cancer of the lung, somatic, 182280 (3)
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| Retinoblastoma, trilateral, 180200 (3)
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| {Leprosy, susceptiblity to, 6} (2)
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| Hypotrichosis 8, 278150 (3)
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| * 609239 LYSOPHOSPHATIDIC ACID RECEPTOR 6| LPAR6
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| {Autism susceptibility 3} (2)
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| Congenital disorder of glycosylation, type Ip, 613661 (3)
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| {Stature QTL 20} (2)
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| Wilson disease, 277900 (3)
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| Spinocerebellar ataxia 8, 608768 (3)
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| * 603680 ATAXIN 8 OPPOSITE STRAND| ATXN8OS
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| ?Breast cancer, type 3 (2)
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| Specific language impairment QTL, 3 (2)
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| Postaxial polydactyly, type A2 (2)
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| Auditory neuropathy, autosomal dominant, 1, 609129 (3)
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| Developmental dysplasia of the hip 1 (2)
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| {Hirschsprung disease, susceptibility to, 2}, 600155 (3)
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| ABCD syndrome, 600501 (3)
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| Waardenburg syndrome, type 4A, 277580 (3)
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| Panic disorder syndrome 1 (2)
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| Ceroid lipofuscinosis, neuronal, 5, 256731 (3)
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| * 609678 SLIT- AND NTRK-LIKE FAMILY, MEMBER 1| SLITRK1
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| Trichotillomania, 613229 (3)
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| Deafness and myopia, 221200 (3)
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| Microcoria, congenital (2)
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| Nystagmus 4, congenital, autosomal dominant (2)
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| Feingold syndrome 2, 614326 (3)
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| Photoparoxysmal response 2 (2)
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| Mitral valve prolapse, myxomatous 3 (2)
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| Omodysplasia 1, 258315 (3)
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| Keratoconus 7 (2)
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| * 232000 PROPIONYL-CoA CARBOXYLASE, ALPHA SUBUNIT| PCCA
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| {Schizophrenia}, 181500 (2)
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| {Systemic lupus erythematosus, susceptibility to, 5} (2)
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| Holoprosencephaly-5, 609637 (3)
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